Kidney cancer in children
In keeping with September as the childhood cancer month, I discuss a common childhood cancer of the kidney called Wilms tumour, or nephroblastoma.
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It is the most common childhood abdominal cancer in childhood.
Wilms tumour is thought to be caused by alterations of genes responsible for normal development of the genital and the urinary systems.
Proof of this stems from observation that Wilms tumour tends to occur in the presence of common abnormalities of the genitourinary system such as undescended testes, horseshoe kidneys and abnormal opening on the penile shaft called hypospadias.
Wilms tumour affects approximately 10 children and adolescents per 1 million before age 15 .. Commonly, one kidney is affected but in about five -10 per cent of patients, both kidneys are affected at the same time or one after the other.
Wilms tumour appears to be relatively more common in Africa and least common in East Asia. It is relatively more common in blacks than in whites. It is more seen in females than males.
The median age at diagnosis of Wilms tumour is approximately three to five years.
The most common manifestation of Wilms tumour is an asymptomatic abdominal swelling. The mass is painless and is usually felt accidentally by parents. In about 80 per cent of cases, abdominal swelling is the presenting complaint.
However, less common symptoms include passage of bloody urine (haematuria) and infections along the pathway of voiding urine (urinary tract infections). A few patients may bleed into their tumour and
present with low blood pressure, anaemia, and fever.
Rarely patients with advanced disease may present with symptoms related to spread to the lungs. Unexplained weight loss with the abdominal mass is a big clue for this cancer.
Examination by a doctor often reveals an abdominal mass large enough to be felt. It is worth emphasising that once the mass is felt, parents should avoid frequent examination of it as it could lead to the rupture of a large tumour into other abdominal structures causing it to spread.
Once confirmed the doctor would look for other associations such as abnormalities of the eyes and abnormal opening of the penile shaft in males.
The following laboratory investigations are indicated in patients with Wilms tumour:
Full blood count
Chemistry profile - Including kidney function tests and liver function test
Urinalysis, stool examination and lumbar puncture Coagulation studies and in the advanced worlds, cytogenetics studies
Bone marrow examination
Patients with suspected lung lesions will need chest radiography
Renal ultrasonography is often the initial study, because it does not expose children to the detrimental effects of radiation. Abdominal computed tomography (CT) scanning helps in determining the origin of the tumour as well as the spread of the disease. Abdominal magnetic resonance imaging (MRI) is reportedly the most sensitive imaging modality for determination of spread into the large blood vessels.
Fortunately, this is one of the tumours that if seen early can be completely cured. Treatment is multidisciplinary. It involves a paediatric cancer specialist (oncologist), a paediatric surgeon as well as a radiotherapist.
Depending on the state, chemotherapy- using drugs to kill the cancer cells is done. This reduces the size of the tumour and makes it very easy for surgery to remove the affected kidney.
Chemotherapy is continued after the surgery after which radiotherapy is done to take care of those that have spread to distant sites.
Approximately 80-90 per cent of children with a diagnosis of Wilms tumour survive with current multimodality therapy. This contrasts with the rate of 10 per cent some 50 years ago. The addition of radiation therapy to surgery alone improved survival rates to approximately 40 per cent . With the use of chemotherapy, survival rates have doubled.
Surgery is done to remove the diseased kidney leaving the child with one functional kidney. In almost all patients, the remaining kidney can compensate and maintain adequate kidney function.
The most important way to survive this cancer is for it to be diagnosed early, treatment instituted early and the long follow up regime strictly adhered to.
Refreshingly, this cancer can easily be treated at the cancer unit of the Children’s Block, Korle-Bu Teaching Hospital and the country abounds with so many success stories.
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A member of Paediatric Society of Ghana